Suppr超能文献

平山病的神经电生理特征:14 例报告。

Neuroelectrophysiological characteristics of Hirayama disease: report of 14 cases.

机构信息

Department of Neurology, First Affiliated Hospital, Chongqing Medical University, Chongqing 400016, China.

出版信息

Chin Med J (Engl). 2012 Jul;125(14):2440-3.

Abstract

BACKGROUND

Hirayama disease is a juvenile muscular atrophy of the distal upper extremities and affects mainly young males. The present study aimed to investigate the neuroelectrophysiological characteristics of Hirayama disease.

METHODS

We retrospectively analyzed the neural conduction velocity (NCV) parameters and needle-electrode electromyograms (EMG) of 14 patients with Hirayama disease. According to the clinical features of the patients, NCV was performed on affected upper-limb including median nerves and ulnar nerves, while EMG was selectively performed on upper and lower extremities, sternocleidomast and thoracic paraspinal muscles.

RESULTS

The median nerves of all affected upper limbs of patients with Hirayama disease had normal conduction velocities and compound motor action potentials (CMAPs). The ulnar nerves of all affected upper limbs also had normal conduction velocities. Of the 16 measured ulnar nerves of the affected upper limbs, eight had normal CMAPS, while the other eight showed CMAPs below the normal value by < 20%. All patients had neurogenic injury on the affected side in muscles innervated by anterior horn cells at the lower cervical region (C7-8, T1). Four patients had unilateral upper-limb muscle neurogenic injury on the affected side. Seven patients had bilateral upper-limb muscle neurogenic injury, while only two patients experienced bilateral upper-limb muscle atrophy/weakness. The other three patients showed extensive neurogenic injury (unilateral upper-limb muscle atrophy/weakness in one patient, bilateral symptoms in the other two patients).

CONCLUSIONS

Electromyographic examination showed that the majority of Hirayama disease patients exhibited characteristic segmental injury in the anterior horn of the lower cervical region, while a few patients exhibited extensive neurogenic injury. These data suggest that the actual influence of Hirayama disease may be more extensive than indicated by the clinical presentations.

摘要

背景

平山病是一种青少年远端上肢肌萎缩症,主要影响年轻男性。本研究旨在探讨平山病的神经电生理特征。

方法

我们回顾性分析了 14 例平山病患者的神经传导速度(NCV)参数和针电极肌电图(EMG)。根据患者的临床特征,对受累上肢的正中神经和尺神经进行 NCV 检查,而 EMG 则选择性地在上肢、下肢、胸锁乳突肌和胸段棘旁肌进行。

结果

所有平山病患者受累上肢的正中神经传导速度和复合运动动作电位(CMAP)均正常。所有受累上肢的尺神经传导速度也正常。在 16 条受累上肢的测量尺神经中,8 条的 CMAP 正常,而另外 8 条的 CMAP 值低于正常 20%以下。所有患者在下颈段(C7-8、T1)的前角细胞支配的受累侧肌肉均出现神经源性损伤。4 例患者出现受累侧单侧上肢肌肉神经源性损伤。7 例患者出现双侧上肢肌肉神经源性损伤,而仅 2 例患者出现双侧上肢肌肉萎缩/无力。另外 3 例患者表现为广泛的神经源性损伤(1 例患者出现单侧上肢肌肉萎缩/无力,另外 2 例患者出现双侧症状)。

结论

肌电图检查显示,大多数平山病患者在前角出现特征性的节段性损伤,而少数患者出现广泛的神经源性损伤。这些数据表明,平山病的实际影响可能比临床表现所表明的更为广泛。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验